PMID- 25512144 OWN - NLM STAT- MEDLINE DCOM- 20170110 LR - 20181113 IS - 1436-3305 (Electronic) IS - 1436-3291 (Linking) VI - 19 IP - 1 DP - 2016 Jan TI - HER2 testing in paired biopsy and excision specimens of gastric cancer: the reliability of the scoring system and the clinicopathological factors relevant to discordance. PG - 176-82 LID - 10.1007/s10120-014-0453-0 [doi] AB - BACKGROUND: Inclusion of trastuzumab in chemotherapy regimens is advantageous for patients with advanced or metastatic gastric cancer who overexpress HER2. Therefore, accurate assessment of HER2 status in tumor tissue is critical when weighing treatment options. METHODS: We examined HER2 expression in 180 paired endoscopic biopsy and surgical excision specimens of gastric cancers via immunohistochemistry (IHC). Equivocal IHC results (IHC 2+) were resolved by HER2 fluorescence in situ hybridization (FISH). The relationships of several clinical and pathological features with discordant HER2 results in paired specimens were determined. RESULTS: Fourteen biopsy specimens and surgical specimens (7.8%) were HER2-positive. Discordant HER2 IHC scores were observed in 90 paired specimens (50%) and 8 paired specimens (4.4%) had discordant results. The kappa coefficients for an HER2 diagnostic algorithm were 0.264, 0.339, and 0.690 for IHC scores, IHC categories, and final results, respectively (p < 0.001). Discordant HER2 results were significantly associated with discordant tumor differentiation in the paired biopsy and excision specimens (p = 0.01). Intratumoral heterogeneity did not predict HER2 discordance. There was no association between HER2 discordance and the number of biopsy tissue fragments (p = 0.764). CONCLUSIONS: Hofmann's HER2 scoring system is a fairly reliable tool for evaluating HER2 status in biopsy and excision specimens. Discordant HER2 results in paired specimens were observed in a small percentage of gastric cancers. Testing all available specimens should be considered in order to eliminate discrepancies, especially when discordant tumor differentiation is observed. FAU - Huang, Shih-Chiang AU - Huang SC AD - Department of Anatomical Pathology, Chang Gung Memorial Hospital, Chang Gung University, College of Medicine, Taoyuan, Taiwan, ROC. FAU - Ng, Kwai-Fong AU - Ng KF AD - Department of Anatomical Pathology, Chang Gung Memorial Hospital, Chang Gung University, College of Medicine, Taoyuan, Taiwan, ROC. FAU - Lee, Shang-En AU - Lee SE AD - Cancer Diagnostic Laboratory, Chang Gung Memorial Hospital, Taoyuan, Taiwan, ROC. FAU - Chen, Kuang-Hua AU - Chen KH AD - Department of Anatomical Pathology, Chang Gung Memorial Hospital, Chang Gung University, College of Medicine, Taoyuan, Taiwan, ROC. FAU - Yeh, Ta-Sen AU - Yeh TS AD - Department of Surgery, Chang Gung Memorial Hospital, Chang Gung University, College of Medicine, Taoyuan, Taiwan, ROC. FAU - Chen, Tse-Ching AU - Chen TC AD - Department of Anatomical Pathology, Chang Gung Memorial Hospital, Chang Gung University, College of Medicine, Taoyuan, Taiwan, ROC. ctc323@cgmh.org.tw. AD - Department of Pathology, Chang Gung Memorial Hospital, No. 5 Fuxing St., Guishan Township, Taoyuan County, 333, Taiwan, ROC. ctc323@cgmh.org.tw. LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20141217 PL - Japan TA - Gastric Cancer JT - Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association JID - 100886238 RN - 0 (Biomarkers, Tumor) RN - EC 2.7.10.1 (ERBB2 protein, human) RN - EC 2.7.10.1 (Receptor, ErbB-2) SB - IM MH - Adult MH - Aged MH - Aged, 80 and over MH - Biomarkers, Tumor MH - Biopsy/*methods MH - Endoscopy, Gastrointestinal MH - Female MH - Humans MH - Immunohistochemistry/*methods MH - In Situ Hybridization, Fluorescence/methods MH - Male MH - Middle Aged MH - Receptor, ErbB-2/*analysis/genetics/metabolism MH - Retrospective Studies MH - Stomach Neoplasms/metabolism/*pathology/surgery OTO - NOTNLM OT - Biopsy OT - Discordance OT - Excision OT - Gastric cancer OT - HER2 EDAT- 2014/12/17 06:00 MHDA- 2017/01/11 06:00 CRDT- 2014/12/17 06:00 PHST- 2014/07/16 00:00 [received] PHST- 2014/11/28 00:00 [accepted] PHST- 2014/12/17 06:00 [entrez] PHST- 2014/12/17 06:00 [pubmed] PHST- 2017/01/11 06:00 [medline] AID - 10.1007/s10120-014-0453-0 [pii] AID - 10.1007/s10120-014-0453-0 [doi] PST - ppublish SO - Gastric Cancer. 2016 Jan;19(1):176-82. doi: 10.1007/s10120-014-0453-0. Epub 2014 Dec 17.